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LRRK2 antibody (AA 878-909)

The Rabbit Polyclonal anti-LRRK2 antibody is suitable to detect LRRK2 in samples from Human and Mouse. It has been validated for WB, ELISA and IHC.
Catalog No. ABIN3031607
$612.54
Plus shipping costs $50.00
Shipping to: United States
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Quick Overview for LRRK2 antibody (AA 878-909) (ABIN3031607)

Target

See all LRRK2 Antibodies
LRRK2 (Leucine-Rich Repeat Kinase 2 (LRRK2))

Reactivity

Human, Mouse

Host

  • 7
  • 3
Rabbit

Clonality

  • 7
  • 3
Polyclonal

Conjugate

  • 10
This LRRK2 antibody is un-conjugated

Application

  • 9
  • 4
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Binding Specificity

    • 5
    • 2
    • 2
    • 1
    • 1
    AA 878-909

    Purification

    Antigen affinity purified

    Immunogen

    A portion of amino acids 878-909 from the human protein was used as the immunogen for this LRRK2 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the LRRK2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,IHC (Paraffin): 1:10-1:50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Aliquot the LRRK2 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    LRRK2 (Leucine-Rich Repeat Kinase 2 (LRRK2))

    Alternative Name

    LRRK2

    Background

    Parkinson is the second most common neurodegenerative disease after Alzheimers. About 1 percent of people over the age of 65 and 3 percent of people over the age of 75 are affected by the disease. The mutation is the most common cause of Parkinson's disease identified to date. LRRK2, a genetic mutation, was recently found linked to about 5 percent of inherited cases of Parkinson's disease. By high-resolution recombination mapping and candidate gene sequencing in 46 families, 6 disease-segregating mutations (5 missense and 1 putative splice site mutation). It may be central to the pathogenesis of several major neurodegenerative disorders associated with parkinsonism. LRRK2 belongs to the ROCO protein family and includes a protein kinase domain of the MAPKKK class and several other major functional domains.

    UniProt

    Q5S007

    Pathways

    Regulation of G-Protein Coupled Receptor Protein Signaling, Skeletal Muscle Fiber Development
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